Các bài viết có thể truy cập công khai - Ryan E. MillsTìm hiểu thêm
Có tại một số nơi: 74
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute, British …
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, German Research Foundation, European …
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, British …
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health, German Research Foundation
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1784, 2019
Các cơ quan ủy nhiệm: US National Institutes of Health, National Health and Medical Research …
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
M Byrska-Bishop, US Evani, X Zhao, AO Basile, HJ Abel, AA Regier, ...
Cell 185 (18), 3426-3440. e19, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health, European Molecular Biology Laboratory …
Natural mutagenesis of human genomes by endogenous retrotransposons
RC Iskow, MT McCabe, RE Mills, S Torene, WS Pittard, AF Neuwald, ...
Cell 141 (7), 1253-1261, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ...
Science 372 (6537), eabf7117, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, National Natural Science Foundation of …
Structural variation in the sequencing era
SS Ho, AE Urban, RE Mills
Nature Reviews Genetics 21 (3), 171-189, 2020
Các cơ quan ủy nhiệm: US National Institutes of Health
CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome
PK Todd, SY Oh, A Krans, F He, C Sellier, M Frazer, AJ Renoux, K Chen, ...
Neuron 78 (3), 440-455, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health
Small insertions and deletions (INDELs) in human genomes
JM Mullaney, RE Mills, WS Pittard, SE Devine
Human molecular genetics 19 (R2), R131-R136, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
D Pinto, K Darvishi, X Shi, D Rajan, D Rigler, T Fitzgerald, AC Lionel, ...
Nature biotechnology 29 (6), 512-520, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research …
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health, Danish Council for Independent Research …
A highly annotated whole-genome sequence of a Korean individual
JI Kim, YS Ju, H Park, S Kim, S Lee, JH Yi, J Mudge, NA Miller, D Hong, ...
nature 460 (7258), 1011-1015, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
The 1000 Genomes Project: data management and community access
L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ...
Nature methods 9 (5), 459-462, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ...
Nature genetics 48 (6), 593-599, 2016
Các cơ quan ủy nhiệm: US National Science Foundation, US National Institutes of Health, Australian …
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